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Translational Potential of Metabolomics on Animal Models of Inflammatory Bowel Disease—A Systematic Critical Review

In the development of inflammatory bowel disease (IBD), the gut microbiota has been established as a key factor. Recently, metabolomics has become important for understanding the functional relevance of gut microbial changes in disease. Animal models for IBD enable the study of factors involved in d...

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Autores principales: Knudsen, Lina Almind, Desdorf, Rasmus, Möller, Sören, Sørensen, Signe Bek, Hansen, Axel Kornerup, Andersen, Vibeke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7312423/
https://www.ncbi.nlm.nih.gov/pubmed/32485793
http://dx.doi.org/10.3390/ijms21113856
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author Knudsen, Lina Almind
Desdorf, Rasmus
Möller, Sören
Sørensen, Signe Bek
Hansen, Axel Kornerup
Andersen, Vibeke
author_facet Knudsen, Lina Almind
Desdorf, Rasmus
Möller, Sören
Sørensen, Signe Bek
Hansen, Axel Kornerup
Andersen, Vibeke
author_sort Knudsen, Lina Almind
collection PubMed
description In the development of inflammatory bowel disease (IBD), the gut microbiota has been established as a key factor. Recently, metabolomics has become important for understanding the functional relevance of gut microbial changes in disease. Animal models for IBD enable the study of factors involved in disease development. However, results from animal studies may not represent the human situation. The aim of this study was to investigate whether results from metabolomics studies on animal models for IBD were similar to those from studies on IBD patients. Medline and Embase were searched for relevant studies up to May 2017. The Covidence systematic review software was used for study screening, and quality assessment was conducted for all included studies. Data showed a convergence of ~17% for metabolites differentiated between IBD and controls in human and animal studies with amino acids being the most differentiated metabolite subclass. The acute dextran sodium sulfate model appeared as a good model for analysis of systemic metabolites in IBD, but analytical platform, age, and biological sample type did not show clear correlations with any significant metabolites. In conclusion, this systematic review highlights the variation in metabolomics results, and emphasizes the importance of expanding the applied detection methods to ensure greater coverage and convergence between the various different patient phenotypes and animal models of inflammatory bowel disease.
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spelling pubmed-73124232020-06-26 Translational Potential of Metabolomics on Animal Models of Inflammatory Bowel Disease—A Systematic Critical Review Knudsen, Lina Almind Desdorf, Rasmus Möller, Sören Sørensen, Signe Bek Hansen, Axel Kornerup Andersen, Vibeke Int J Mol Sci Review In the development of inflammatory bowel disease (IBD), the gut microbiota has been established as a key factor. Recently, metabolomics has become important for understanding the functional relevance of gut microbial changes in disease. Animal models for IBD enable the study of factors involved in disease development. However, results from animal studies may not represent the human situation. The aim of this study was to investigate whether results from metabolomics studies on animal models for IBD were similar to those from studies on IBD patients. Medline and Embase were searched for relevant studies up to May 2017. The Covidence systematic review software was used for study screening, and quality assessment was conducted for all included studies. Data showed a convergence of ~17% for metabolites differentiated between IBD and controls in human and animal studies with amino acids being the most differentiated metabolite subclass. The acute dextran sodium sulfate model appeared as a good model for analysis of systemic metabolites in IBD, but analytical platform, age, and biological sample type did not show clear correlations with any significant metabolites. In conclusion, this systematic review highlights the variation in metabolomics results, and emphasizes the importance of expanding the applied detection methods to ensure greater coverage and convergence between the various different patient phenotypes and animal models of inflammatory bowel disease. MDPI 2020-05-29 /pmc/articles/PMC7312423/ /pubmed/32485793 http://dx.doi.org/10.3390/ijms21113856 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Knudsen, Lina Almind
Desdorf, Rasmus
Möller, Sören
Sørensen, Signe Bek
Hansen, Axel Kornerup
Andersen, Vibeke
Translational Potential of Metabolomics on Animal Models of Inflammatory Bowel Disease—A Systematic Critical Review
title Translational Potential of Metabolomics on Animal Models of Inflammatory Bowel Disease—A Systematic Critical Review
title_full Translational Potential of Metabolomics on Animal Models of Inflammatory Bowel Disease—A Systematic Critical Review
title_fullStr Translational Potential of Metabolomics on Animal Models of Inflammatory Bowel Disease—A Systematic Critical Review
title_full_unstemmed Translational Potential of Metabolomics on Animal Models of Inflammatory Bowel Disease—A Systematic Critical Review
title_short Translational Potential of Metabolomics on Animal Models of Inflammatory Bowel Disease—A Systematic Critical Review
title_sort translational potential of metabolomics on animal models of inflammatory bowel disease—a systematic critical review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7312423/
https://www.ncbi.nlm.nih.gov/pubmed/32485793
http://dx.doi.org/10.3390/ijms21113856
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